Canonical Allele Identifier: CA1167985699
Gene: PCSK9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55061452C= , CM000663.2:g.55061452C= GRCh38
NC_000001.10:g.55527125C= , CM000663.1:g.55527125C= GRCh37
NC_000001.9:g.55299713C= NCBI36
NG_009061.1:g.26906C= , LRG_275:g.26906C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.*99C= ENSP00000501161.2:n.*99C=
ENST00000710286.1:c.2116C= ENSP00000518176.1:p.Gln706=
ENST00000673903.1:c.1384C= ENSP00000501257.1:p.Gln462=
ENST00000673913.1:c.609C= ENSP00000501161.1:n.609C=
ENST00000302118.5:c.1759C= MANE Select ENSP00000303208.5:p.Gln587=
ENST00000490692.1:n.2305C=
NM_174936.3:c.1759C= , LRG_275t1:c.1759C= NP_777596.2:p.Gln587=
NR_110451.1:n.1366C=
XM_011541193.1:c.880C= XP_011539495.1:p.Gln294=
NM_174936.4:c.1759C= MANE Select NP_777596.2:p.Gln587=
NR_110451.2:n.1366C=